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[Cancer Research 52, 117-120, January 1, 1992]
© 1992 American Association for Cancer Research

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Interaction of Photodynamic Treatment and Either Hyperthermia or Ionizing Radiation and of Ionizing Radiation and Hyperthermia with Respect to Cell Killing of L929 Fibroblasts, Chinese Hamster Ovary Cells, and T24 Human Bladder Carcinoma Cells1

Carla Prinsze, Louis C. Penning, Tom M. A. R. Dubbelman and John VanSteveninck2

Department of Medical Biochemistry, Sylvius Laboratories, P. O. Box 9503, 2300 RA Leiden, The Netherlands

Both hyperthermia and photodynamic therapy of cancer are frequently used in combination with other treatment modalities in order to improve tumor control with minimal damage to normal tissues. The present results indicate that the most effective combination of treatment modalities is different in different cell types. For instance, ionizing irradiation and hyperthermia exhibited additivity when applied to L929 fibroblasts, in contrast to the synergistic interaction described before in many other cell lines. This aberrant behavior of L929 cells could be explained by the relative insensitivity of DNA repair in these cells to hyperthermia. Conversely, a synergistic interaction between photodynamic treatment and ionizing irradiation was observed with L929 fibroblasts, whereas these treatments were additive with Chinese hamster ovary and T24 cells. The synergistic interaction with L929 cells could be explained by the high sensitivity of DNA repair in these cells to photodynamic treatment. Photodynamic treatment and hyperthermia exhibited a synergistic interaction in L929, Chinese hamster ovary, and T24 cells. The critical target for cell killing by the combined treatment protocol in these cell lines has not yet been elucidated. In all three cell lines, however, analysis of the results according to the Arrhenius equation revealed a photodynamically induced change of both the frequency factor and the activation energy of subsequent thermal cell killing. It is considered that this may indicate a basic mechanism, in which a particular protein is a common, critical target of the two modalities of treatment.

1 This work was supported by the Netherlands Cancer Foundation (Grant IKW 89-01).

2 To whom requests for reprints should be addressed.

Received 1/14/91. Accepted 10/21/91.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Cell Growth & Differentiation
Copyright © 1992 by the American Association for Cancer Research.